Hydrochloric Acid → HCID 86611689, compound
Reaction equation
[NH:1]([CH:4]([C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1)[N:5]1[CH2:10][CH2:9][N:8](C(OC(C)(C)C)=O)[CH2:7][CH2:6]1)[C:2]#[N:3].[ClH:24]>O1CCOCC1>[ClH:24].[C:18]1([C:4](=[N:1][C:2]#[N:3])[N:5]2[CH2:6][CH2:7][NH:8][CH2:9][CH2:10]2)[CH:19]=[CH:20][CH:21]=[CH:22][CH:23]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
tert-Butyl 4-(cyanamido(phenyl)methyl)piperazine-1-carboxylate (1.5 g) was dissolved in 16 ml of 2M HCl in dioxane. After four hours, the solution was diluted with dioxane (20 ml) and the solid, (phenyl(piperazin-1-yl)methylene)cyanamide hydrochloride (1 g), was collected via filtration. It was washed with ether before further use.
Workup
- filtrationthe solid, (phenyl(piperazin-1-yl)methylene)cyanamide hydrochloride (1 g), was collected via filtration
- washIt was washed with ether before further use
Sources & evidence
- ORD record
- ord-9b98787018c34b8493358f967ea80a46
- Source dataset
- uspto-grants-2008_07
- Patent number
- US07396830B2
Reaction notes
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